NCT06872060

Brief Summary

This study will investigating the effects of glucagon on renal blood flow in humans using MRI technology. Glucagon, a hormone produced by the pancreas, plays a key role in regulating blood sugar levels. It has been shown to affect renal function, including electrolyte balance and blood flow, especially in conditions like type 2 diabetes where abnormal glucagon levels are common. The study aims to understand how glucagon affects regional blood flow in the kidneys, specifically the cortex and medulla, and whether these effects are mediated by glucagon receptors. The study will be conducted on 10 healthy male participants aged 20-60 years. It involves three test days where participants will receive either glucagon, glucagon with a GLP-1 receptor antagonist, or placebo. Blood flow, glomerular filtration rate, and other renal functions will be measured using MRI. The study seeks to clarify whether glucagon's effects on the kidneys are linked to changes in regional blood flow and to determine if these effects are mediated solely by glucagon receptors.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
17mo left

Started Jun 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 21, 2025

Completed
19 days until next milestone

First Posted

Study publicly available on registry

March 12, 2025

Completed
1.2 years until next milestone

Study Start

First participant enrolled

June 1, 2026

Expected
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2027

Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2027

Last Updated

October 3, 2025

Status Verified

September 1, 2025

Enrollment Period

1.4 years

First QC Date

February 21, 2025

Last Update Submit

September 29, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Blood perfusion of the kidney

    we would like to measure blood perfusion of the kidneys over time

    7 measurements of 10 minutes each from the start of infusion (time 0) and up to one hour (time 60).

Secondary Outcomes (2)

  • Blood flow of the renal arteries

    7 measurements of 10 minutes each from the start of infusion (time 0) and up to one hour (time 60).

  • blood oxygen saturation of the kidneys

    7 measurements of 10 minutes each from the start of infusion (time 0) and up to one hour (time 60).

Study Arms (3)

Glucagon

EXPERIMENTAL
Drug: GlucagonDrug: Glucagon+Exendin9-39Drug: Sodium chloride

Glucagon+Exendin9-39

EXPERIMENTAL
Drug: GlucagonDrug: Glucagon+Exendin9-39Drug: Sodium chloride

Sodium chloride (Placebo comparator)

PLACEBO COMPARATOR
Drug: GlucagonDrug: Glucagon+Exendin9-39Drug: Sodium chloride

Interventions

Glucagon infusion at 5 ng·kg-¹·min-¹ from 0-30 minutes and 10 ng·kg-¹·min-¹ from 30-60 minutes.

GlucagonGlucagon+Exendin9-39Sodium chloride (Placebo comparator)

Glucagon infusion at 5 ng·kg-¹·min-¹ from 0-30 minutes and 10 ng·kg-¹·min-¹ from 30-60 minutes, plus a GLP-1R antagonist, exendin 9-39 (900 pmol·kg-¹·min-¹), given intravenously from -30 to 60 minutes

GlucagonGlucagon+Exendin9-39Sodium chloride (Placebo comparator)

Placebo (0.9% NaCl).

GlucagonGlucagon+Exendin9-39Sodium chloride (Placebo comparator)

Eligibility Criteria

Age20 Years - 60 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Normal health confirmed through; Interview and Medical examination
  • Normal values with respect to blood concentrations of fasting plasma glucose, fasting plasma total cholesterol, fasting triglycerides, HDL, LDL, creatinine, liver function tests, and electrolytes
  • Informed consent

You may not qualify if:

  • Immunosuppressive treatment in the previous 12 months
  • Alcohol abuse
  • Medical treatment with oral glucocorticoids, dipeptidyl peptidase-4 (DPP-4) inhibitors, or GLP-1 receptor agonists, which, in the opinion of the principal investigator, may interfere with glucose metabolism
  • Use of lithium
  • Medical treatment that affects insulin secretion or the renin-angiotensin-aldosterone system
  • Liver disease (ALT \> 2x normal value)
  • Renal impairment (serum creatinine \> 130 µM and/or albuminuria)
  • Individuals with severe claustrophobia
  • Individuals with MR-incompatible foreign bodies
  • Individuals with hypertension

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Kidney Diseases

Interventions

GlucagonSodium Chloride

Condition Hierarchy (Ancestors)

Urologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital Diseases

Intervention Hierarchy (Ancestors)

ProglucagonPancreatic HormonesPeptide HormonesHormonesHormones, Hormone Substitutes, and Hormone AntagonistsPeptidesAmino Acids, Peptides, and ProteinsChloridesHydrochloric AcidChlorine CompoundsInorganic ChemicalsSodium Compounds

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief Physician, Associate Professor, PhD, MD

Study Record Dates

First Submitted

February 21, 2025

First Posted

March 12, 2025

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

November 1, 2027

Study Completion (Estimated)

November 1, 2027

Last Updated

October 3, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share